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FDA 510(k)

MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS

K-Number: K924284 · 1993-02-10

ApplicantMicromec Surgical, Inc.
Decision Date1993-02-10
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Micromec Surgical, Inc.. It received FDA 510(k) clearance on 1993-02-10 under 510(k) number K924284. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS?

MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1993-02-10. The listed applicant is Micromec Surgical, Inc.. The 510(k) number is K924284.

When did MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS receive FDA 510(k) clearance?

MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS received FDA 510(k) clearance on 1993-02-10, under 510(k) number K924284.

Who is the listed applicant for MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS?

The FDA 510(k) record lists Micromec Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS?

The FDA product code for MICROSURGE DIRECTOR ARTICULATING INSTRUMENTS is GCJ.

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Related Devices (Code: GCJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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